Canonical Allele Identifier: PA105899
Gene: KRT17 HGNC NCBI

Linked Data

ClinVar Variation Id: 14588
ClinVar RCV Id: RCV000015690 RCV000056521
JSON-LD

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_000413.1:p.Tyr98Asp
CA216620
NM_000422.3:c.292T>G